Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:43407727-43407852 | Common:1; Rare:49 | ||||
chr10:43408779-43408937 | Rare:52 | ||||
chr10:43409129-43409432 | Common:3; Rare:105 | ||||
chr10:43574554-43574698 | Common:1; Rare:58 | ||||
chr10:43606369-43606491 | Common:3; Rare:39 | ||||
chr10:43648800-43648980 | Common:1; Rare:52 | ||||
chr10:44385084-44385273 | Rare:59 | ||||
chr10:44959555-44959815 | Common:2; Rare:82 | ||||
chr10:45000766-45000968 | Common:1; Rare:86 | ||||
chr10:45672757-45672879 | Rare:42 | ||||
chr10:45972349-45972691 | Common:5; Rare:111 | ||||
chr10:49539023-49539168 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
chr10:49941904-49942124 | Rare:69 | ||||
chr10:50067786-50067992 | Common:4; Rare:90 | ||||
chr10:50623861-50624084 | Common:1; Rare:84 |